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Pentanoic Acid → Pentanamide

HRID 1657055
ノート
印刷プレビュー

反応式

HRID 1657055 の反応式
[C:1]([OH:7])(=O)[CH2:2][CH2:3][CH2:4][CH3:5].ClC([O:11][CH2:12][CH3:13])=O.[CH2:14]([N:16](CC)CC)C>C(Cl)(Cl)Cl>[CH:12]([O:11][CH:4]([CH3:3])[CH3:5])([CH3:13])[CH3:14].[C:1]([NH2:16])(=[O:7])[CH2:2][CH2:3][CH2:4][CH3:5]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 7991Pentanoic AcidHCID 8471TriethylamineHCID 10928Ethyl chloroformate

生成物 2

HCID 7914Diisopropyl EtherHCID 12298Pentanamide収率 124.9%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

反応条件

温度
-20 °C

実験手順

Valeric acid (10.86 mL, 100 mmol, 1.0 eq) was dissolved in chloroform (100 mL, 0.1 M) and cooled to -20° C. Ethyl chloroformate (9.52 mL, 100 mmol, 1 eq) was added. Triethylamine (14.0 mL, 100 mmol, 1.0 eq) was then added dropwise over 5 minutes. The mixture was stirred at -20° C. for 30 minutes. Ammonia was bubbled through the mixture 10 minutes at -20° C. and 20 minutes at 0° C. The mixture was then allowed to warm to room temperature and stirred for 90 minutes. Chloroform (100 mL) and 1 N hydrochloric acid (50 mL) were added. The layers were separated and the organic layer was washed with saturated sodium bicarbonate solution, dried (magnesium sulfate), filtered and freed of solvent in vacuo. Trituration with isopropyl ether gave the title compound (6.315 g, 62%) as a white solid.

後処理

  1. customAmmonia was bubbled through the mixture 10 minutes at -20° C. and 20 minutes at 0° C
  2. temperatureto warm to room temperature
  3. stirringstirred for 90 minutes
  4. additionChloroform (100 mL) and 1 N hydrochloric acid (50 mL) were added
  5. customThe layers were separated
  6. washthe organic layer was washed with saturated sodium bicarbonate solution
  7. dry with materialdried (magnesium sulfate)
  8. filtrationfiltered

出典と根拠

ORDレコード
ord-0c5f654426d14d94ac0b4fd8e5529c55
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05256695

反応ノート

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